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University of Illinois at Urbana-Champaign

Palladium-Catalyzed Alkenylsilanol Cross -Coupling Reactions: Method Development and Mechanistic Analysis

Abstract

dc:description

The transmetalation mechanism was examined through the natural abundance 13C NMR kinetic isotope effect (KIE) studies. This provided evidence for either palladium-olefin complexation or a Heck-type carbometalation as the turnover-limiting step for these cross-coupling reactions.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2015

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Sweis, Ramzi Farah
Contributors dc:contributor
  • Denmark, Scott E.

Subjects

dc:subject × 1

Rights

Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
(MiAaPQ)AAI3131032
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/84140

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Sweis, Ramzi Farah. Palladium-Catalyzed Alkenylsilanol Cross -Coupling Reactions: Method Development and Mechanistic Analysis. Dissertation thesis, University of Illinois at Urbana-Champaign, 2015. http://hdl.handle.net/2142/84140